L. Chitsulo, D. Engels, A. Montresor, and L. Savioli, The global status of schistosomiasis and its control, Acta Tropica, vol.77, issue.1, pp.41-51, 2000.
DOI : 10.1016/S0001-706X(00)00122-4

L. Chitsulo, P. Loverde, and D. Engels, Focus: Schistosomiasis, Nature Reviews Microbiology, vol.68, issue.1, pp.12-13, 2004.
DOI : 10.1016/S1471-4922(02)02386-3

B. Gryseels, K. Polman, J. Clerinx, and L. Kestens, Human schistosomiasis, The Lancet, vol.368, issue.9541, pp.1106-1118, 2006.
DOI : 10.1016/S0140-6736(06)69440-3

F. Guillou, G. Mitta, R. Galinier, and C. Coustau, Identification and expression of gene transcripts generated during an anti-parasitic response in Biomphalaria glabrata, Developmental & Comparative Immunology, vol.31, issue.7, pp.657-671, 2007.
DOI : 10.1016/j.dci.2006.10.001

URL : https://hal.archives-ouvertes.fr/hal-00170685

A. Bouchut, C. Coustau, B. Gourbal, and G. Mitta, Compatibility in the Biomphalaria glabrata/Echinostoma caproni model: new candidate genes evidenced by a suppressive subtractive hybridization approach, Parasitology, vol.70, issue.04, pp.575-588, 2007.
DOI : 10.1016/S0020-7519(01)00133-3

URL : https://hal.archives-ouvertes.fr/hal-00170741

C. Adema, P. Hanington, C. Lun, G. Rosenberg, and A. Aragon, Differential transcriptomic responses of Biomphalaria glabrata (Gastropoda, Mollusca) to bacteria and metazoan parasites, Schistosoma mansoni and Echinostoma paraensei (Digenea, Platyhelminthes), Molecular Immunology, vol.47, issue.4, pp.849-860, 2010.
DOI : 10.1016/j.molimm.2009.10.019

DOI : 10.1645/GE-193R1

A. Lockyer, J. Spinks, A. Walker, R. Kane, and L. Noble, Biomphalaria glabrata transcriptome: Identification of cell-signalling, transcriptional control and immune-related genes from open reading frame expressed sequence tags (ORESTES), Developmental & Comparative Immunology, vol.31, issue.8, pp.763-782, 2007.
DOI : 10.1016/j.dci.2006.11.004

B. Hanelt, C. Lun, and C. Adema, Comparative ORESTES-sampling of transcriptomes of immune-challenged Biomphalaria glabrata snails, Journal of Invertebrate Pathology, vol.99, issue.2, pp.192-203, 2008.
DOI : 10.1016/j.jip.2008.06.002

A. Lockyer, J. Spinks, R. Kane, K. Hoffmann, and J. Fitzpatrick, Biomphalaria glabrata transcriptome: cDNA microarray profiling identifies resistant- and susceptible-specific gene expression in haemocytes from snail strains exposed to Schistosoma mansoni, BMC Genomics, vol.9, issue.1, pp.634-644, 2008.
DOI : 10.1186/1471-2164-9-634

P. Hanington, M. Forys, J. Dragoo, S. Zhang, and C. Adema, Role for a somatically diversified lectin in resistance of an invertebrate to parasite infection, Proceedings of the National Academy of Sciences, vol.107, issue.49, pp.21087-21092, 2010.
DOI : 10.1073/pnas.1011242107

A. Lockyer, A. Emery, R. Kane, A. Walker, and C. Mayer, Early Differential Gene Expression in Haemocytes from Resistant and Susceptible Biomphalaria glabrata Strains in Response to Schistosoma mansoni, PLoS ONE, vol.4, issue.12, p.23300533, 2012.
DOI : 10.1371/journal.pone.0051102.s002

URL : https://hal.archives-ouvertes.fr/halsde-00771961

E. Deleury, G. Dubreuil, N. Elangovan, E. Wajnberg, and J. Reichhart, Specific versus nonspecific immune responses in an invertebrate species evidenced by a comparative de novo sequencing study, PLoS One, vol.7, p.22427848, 2012.
URL : https://hal.archives-ouvertes.fr/halsde-00700368

A. Bravo, S. Likitvivatanavong, S. Gill, and M. Soberon, Bacillus thuringiensis: A story of a successful bioinsecticide, Insect Biochemistry and Molecular Biology, vol.41, issue.7, pp.423-431, 2011.
DOI : 10.1016/j.ibmb.2011.02.006

M. Soberon, J. Lopez-diaz, and A. Bravo, Cyt toxins produced by Bacillus thuringiensis: A protein fold conserved in several pathogenic microorganisms, Peptides, vol.41, pp.87-93, 2013.
DOI : 10.1016/j.peptides.2012.05.023

R. Boyce, A. Lenhart, A. Kroeger, R. Velayudhan, and B. Roberts, ) for the control of dengue vectors: systematic literature review, Tropical Medicine & International Health, vol.43, issue.5, pp.564-577, 2013.
DOI : 10.1111/tmi.12087

I. Larget and H. De-barjac, Specificity and active principle of Bacillus thuringiensis var. israelensis, Bull Soc Pathol Exot Filiales, vol.74, pp.216-227, 1981.

Y. Gamalat, M. Ahmed, A. Ahmed, and A. Asmaa, Biological studies on Biomphalaria alexandrina snails treated with Furcraea selloa marginata plant (family: Agavaceae) and Bacillus thuringiensis kurstaki (Dipel-2x), Journal of Applied Pharmaceutical Science, vol.01, pp.47-55, 2011.

E. De-oliveira, L. Rabinovitch, R. Monnerat, L. Passos, and V. Zahner, Molecular Characterization of Brevibacillus laterosporus and Its Potential Use in Biological Control, Applied and Environmental Microbiology, vol.70, issue.11, pp.6657-6664, 2004.
DOI : 10.1128/AEM.70.11.6657-6664.2004

S. Singer, T. Bair, T. Hammill, A. Berte, and M. Correa-ochoa, Fermentation and toxin studies of the molluscicidal strains ofBacillus brevis, Journal of Industrial Microbiology, vol.2, issue.2, pp.112-119, 1994.
DOI : 10.1007/BF01584108

D. Texera and J. Vicente-scorza, Studies on a bacterial type resembling bacillus pinotti found in Venezuela with pathogenic action on Australorbis glabratus, Arch Venez Pat Trop Parasitol Med, vol.2, pp.235-243, 1954.

D. Bean-knudsen, L. Uhazy, J. Wagner, and B. Young, Systemic infection of laboratory-reared Biomphalaria glabrata (Mollusca: Gastropoda) with an acid-fast bacillus, Journal of Invertebrate Pathology, vol.51, issue.3, pp.291-293, 1988.
DOI : 10.1016/0022-2011(88)90039-0

R. Cole, C. Richards, and T. Popkin, Novel bacterium infecting an African snail, J Bacteriol, vol.132, pp.950-966, 1977.

W. Weisburg, S. Barns, D. Pelletier, and D. Lane, 16S ribosomal DNA amplification for phylogenetic study., Journal of Bacteriology, vol.173, issue.2, pp.697-703, 1991.
DOI : 10.1128/jb.173.2.697-703.1991

I. Dahlloff, H. Baillie, and S. Kjelleberg, rpoB-Based Microbial Community Analysis Avoids Limitations Inherent in 16S rRNA Gene Intraspecies Heterogeneity, Applied and Environmental Microbiology, vol.66, issue.8, pp.3376-3380, 2000.
DOI : 10.1128/AEM.66.8.3376-3380.2000

D. Mota, F. Gomes, E. Paiva, E. Rosado, A. Seldin et al., Use of rpoB gene analysis for identification of nitrogen-fixing Paenibacillus species as an alternative to the 16S rRNA gene, Letters in Applied Microbiology, vol.55, issue.1, pp.34-40, 2004.
DOI : 10.1046/j.1365-2672.2003.02097.x

D. Mota, F. Gomes, E. Paiva, E. Seldin, and L. , Assessment of the diversity of Paenibacillus species in environmental samples by a novel rpoB-based PCR-DGGE method, FEMS Microbiology Ecology, vol.53, issue.2, pp.317-328, 2005.
DOI : 10.1016/j.femsec.2005.01.017

G. Tomas, E. Marc, S. Michael, N. Monika, and N. Andreas, Development of an 18S rRNA gene targeted PCR based diagnostic for the blue crab parasite Hematodinium sp, pp.61-70, 2002.

K. Tamura, D. Peterson, N. Peterson, G. Stecher, and M. Nei, MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods, Molecular Biology and Evolution, vol.28, issue.10, pp.2731-2739, 2011.
DOI : 10.1093/molbev/msr121

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3203626

M. Kimura, A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences, Journal of Molecular Evolution, vol.206, issue.5, Nov., pp.111-120, 1980.
DOI : 10.1007/BF01731581

K. Tamura, The rate and pattern of nucleotide substitution in Drosophila mitochondrial DNA, Mol Biol Evol, vol.9, pp.814-825, 1992.

A. Mattos, J. Kusel, P. Pimenta, and P. Coelho, Activity of praziquantel on in vitro transformed Schistosoma mansoni sporocysts, Mem??rias do Instituto Oswaldo Cruz, vol.101, issue.1, pp.283-287, 2006.
DOI : 10.1590/S0074-02762006000900044

R. Galinier, J. Portela, Y. Mone, J. Allienne, and H. Henri, Biomphalysin, a new beta pore-forming toxin involved in Biomphalaria glabrata immune defense against Schistosoma mansoni, PLoS Pathog, vol.9, p.23555242, 2013.

R. Murray and E. Stackebrandt, Taxonomic Note: Implementation of the Provisional Status Candidatus for Incompletely Described Procaryotes, International Journal of Systematic Bacteriology, vol.45, issue.1, pp.186-187, 1995.
DOI : 10.1099/00207713-45-1-186

J. Chai, Praziquantel Treatment in Trematode and Cestode Infections: An Update, Infection & Chemotherapy, vol.45, issue.1, pp.32-43, 2013.
DOI : 10.3947/ic.2013.45.1.32

D. Cioli, L. Pica-mattoccia, A. Basso, and A. Guidi, Schistosomiasis control: praziquantel forever?, Molecular and Biochemical Parasitology, vol.195, issue.1, pp.23-29, 2014.
DOI : 10.1016/j.molbiopara.2014.06.002

M. Doenhoff, J. Kusel, G. Coles, and D. Cioli, Resistance of Schistosoma mansoni to praziquantel: is there a problem?, Transactions of the Royal Society of Tropical Medicine and Hygiene, vol.96, issue.5, pp.465-469, 2002.
DOI : 10.1016/S0035-9203(02)90405-0

S. Melman, M. Steinauer, C. Cunningham, L. Kubatko, and I. Mwangi, Reduced Susceptibility to Praziquantel among Naturally Occurring Kenyan Isolates of Schistosoma mansoni, PLoS Neglected Tropical Diseases, vol.68, issue.4, 2009.
DOI : 10.1371/journal.pntd.0000504.g004

W. Jobin, F. Ferguson, and J. Palmer, Control of schistosomiasis in Guayama and Arroyo, Bull World Health Organ, vol.42, pp.151-156, 1970.

B. Saladin, K. Saladin, B. Holzer, E. Dennis, and A. Hanson, A pilot control trial of schistosomiasis in central Liberia by mass chemotherapy of target populations, combined with focal application of molluscicide, Acta Trop, vol.40, pp.271-295, 1983.

P. Coura-filho, N. Mendes, C. De-souza, and J. Pereira, The prolonged use of niclosamide as a molluscicide for the control of Schistosoma mansoni, Revista do Instituto de Medicina Tropical de S??o Paulo, vol.34, issue.5, pp.427-431, 1992.
DOI : 10.1590/S0036-46651992000500009

H. Kariuki, H. Madsen, J. Ouma, A. Butterworth, and D. Dunne, Long term study on the effect of mollusciciding with niclosamide in stream habitats on the transmission of schistosomiasis mansoni after community-based chemotherapy in Makueni District, Kenya, Parasites & Vectors, vol.6, issue.1, 2013.
DOI : 10.1186/1756-3305-3-84

J. Dai, Y. Li, W. Wang, Y. Xing, and G. Qu, Resistance to niclosamide in Oncomelania hupensis, the intermediate host of Schistosoma japonicum: should we be worried?, Parasitology, vol.24, issue.02, pp.1-9, 2014.
DOI : 10.1016/S0065-308X(10)72006-6

A. Harrison, The effects of Bayluscid on gastropod snails and other Aquatic Fauna in Rhodesia, Hydrobiologia, vol.25, issue.3-4, pp.371-384, 1966.
DOI : 10.1007/BF00130390

C. Souza, Molluscicide control of snail vectors of schistosomiasis, Mem??rias do Instituto Oswaldo Cruz, vol.90, issue.2, pp.165-168, 1995.
DOI : 10.1590/S0074-02761995000200007

E. Oliveira-filho and F. Paumgartten, Toxicity of Euphorbia milii Latex and Niclosamide to Snails and Nontarget Aquatic Species, Ecotoxicology and Environmental Safety, vol.46, issue.3, pp.342-350, 2000.
DOI : 10.1006/eesa.2000.1924

O. Zinada, Effect of niclosamide on the marketable fish Liza ramada (Risso, 1826) concerning accumulation in muscles and activities of three metabolic liver enzymes, J Egypt Soc Parasitol, vol.30, pp.791-797, 2000.

K. Xiao, X. Zhao, Z. Liu, B. Zhang, and L. Fang, Polychlorinated dibenzo-p-dioxins and dibenzofurans in blood and breast milk samples from residents of a schistosomiasis area with Na-PCP application in China, Chemosphere, vol.79, issue.7, pp.740-744, 2010.
DOI : 10.1016/j.chemosphere.2010.02.042

H. Shoeb, A. Hassan, M. Sayed, and L. Refahy, The molluscicidal properties of Agave decepiens and Agave americana (var. marginata), J Egypt Soc Parasitol, vol.14, pp.265-273, 1984.

K. Chifundera, B. Baluku, and B. Mashimango, Phytochemical Screening and Molluscicidal Potency of Some Zairean Medicinal Plants, Pharmacological Research, vol.28, issue.4, pp.333-340, 1993.
DOI : 10.1006/phrs.1993.1135

V. Schall, M. De-vasconcellos, C. De-souza, and D. Baptista, The molluscicidal activity of Crown of Christ (Euphorbia splendens var. hislopii) latex on snails acting as intermediate hosts of Schistosoma mansoni and Schistosoma haematobium, Am J Trop Med Hyg, vol.58, pp.7-10, 1998.

M. Radwan, S. El-zemity, S. Mohamed, and S. Sherby, Potential of some monoterpenoids and their new N-methyl carbamate derivatives against Schistosomiasis snail vector, Biomphalaria alexandrina, Ecotoxicology and Environmental Safety, vol.71, issue.3, pp.889-894, 2008.
DOI : 10.1016/j.ecoenv.2007.07.002

M. Tadros, N. Ghaly, and M. Moharib, Molluscicidal and schistosomicidal activities of a steroidal saponin containing fraction from Dracaena fragrans (L.), J Egypt Soc Parasitol, vol.38, pp.585-598, 2008.

H. Zhang, H. Xu, Z. Song, L. Chen, and H. Wen, Molluscicidal activity of Aglaia duperreana and the constituents of its twigs and leaves, Fitoterapia, vol.83, issue.6, pp.1081-1086, 2012.
DOI : 10.1016/j.fitote.2012.05.003

K. Singh, D. Singh, and V. Singh, Characterization of the molluscicidal activity of Bauhinia variegata and Mimusops elengi plant extracts against the fasciola vector lymnaea acuminata, Revista do Instituto de Medicina Tropical de S??o Paulo, vol.54, issue.3, pp.135-140, 2012.
DOI : 10.1590/S0036-46652012000300004

Y. Diab, E. Ioannou, A. Emam, C. Vagias, and V. Roussis, Desmettianosides A and B, bisdesmosidic furostanol saponins with molluscicidal activity from Yucca desmettiana, Steroids, vol.77, issue.6, pp.686-690, 2012.
DOI : 10.1016/j.steroids.2012.02.014

C. Dias, K. Rodrigues, F. Carvalho, S. Carneiro, and J. Maia, from Brazil, Chemistry & Biodiversity, vol.98, issue.6, pp.1133-1141, 2013.
DOI : 10.1002/cbdv.201200292

URL : https://hal.archives-ouvertes.fr/insu-00401942

J. Bagalwa, L. Voutquenne-nazabadioko, C. Sayagh, and A. Bashwira, Evaluation of the biological activity of the molluscicidal fraction of Solanum sisymbriifolium against non target organisms, Fitoterapia, vol.81, issue.7, pp.767-771, 2010.
DOI : 10.1016/j.fitote.2010.04.003

L. Rapado, A. Pinheiro, P. Lopes, H. Fokoue, and M. Scotti, Schistosomiasis Control Using Piplartine against Biomphalaria glabrata at Different Developmental Stages, PLoS Neglected Tropical Diseases, vol.60, issue.6, p.23755312, 2013.
DOI : 10.1371/journal.pntd.0002251.s006

W. Jobin, F. Ferguson, and L. Berrios-duran, Effect of Marisa cornuarietis on populations of Biomphalaria glabrata in farm ponds of Puerto Rico, Am J Trop Med Hyg, issue.2, 1973.

G. Perera-de-puga, M. Cong, J. Ferrer, A. Gutierrez, and J. Sanchez, Importance of Tarebia granifera in the control of a population of Biomphalaria peregrina introduced in Cuba, Rev Cubana Med Trop, vol.46, pp.20-24, 1994.

M. Giboda, E. Malek, and R. Correa, Human schistosomiasis in Puerto Rico: reduced prevalence rate and absence of Biomphalaria glabrata, Am J Trop Med Hyg, vol.57, pp.564-568, 1997.

J. Pointier and J. Jourdane, Biological control of the snail hosts of schistosomiasis in areas of low transmission: the example of the Caribbean area, Acta Tropica, vol.77, issue.1, pp.53-60, 2000.
DOI : 10.1016/S0001-706X(00)00123-6

C. Guimaraes, C. Souza, and D. Soares, Possible competitive displacement of planorbids by Melanoides tuberculata in Minas Gerais, Brazil, Mem??rias do Instituto Oswaldo Cruz, vol.96, pp.173-176, 2001.
DOI : 10.1590/S0074-02762001000900027

J. Pointier, Invading freshwater snails and biological control in Martinique Island, French West Indies, Mem??rias do Instituto Oswaldo Cruz, vol.96, pp.67-74, 2001.
DOI : 10.1590/S0074-02762001000900009

URL : http://www.scielo.br/pdf/mioc/v96s0/14x.pdf

A. Giovanelli, C. Da-silva, G. Leal, and D. Baptista, Habitat preference of freshwater snails in relation to environmental factors and the presence of the competitor snail Melanoides tuberculatus (M??ller, 1774), Mem??rias do Instituto Oswaldo Cruz, vol.100, issue.2, pp.169-176, 2005.
DOI : 10.1590/S0074-02762005000200010

I. Sohn and L. Kornicker, Predation of Schistosomiasis Vector Snails by Ostracoda (Crustacea), Science, vol.175, issue.4027, pp.1258-1259, 1972.
DOI : 10.1126/science.175.4027.1258

W. Sodeman, G. Rodrick, and A. Vincent, Lampyridae larva: a natural predator of schistosome vector snails in Liberia, Am J Trop Med Hyg, vol.29, pp.319-7369451, 1980.

R. Consoli, C. Guimaraes, J. Do-carmo, D. Soares, and J. Santos, Astronotus ocellatus (Cichlidae: Pisces) and Macropodus opercularis (Anabatidae: Pisces) as predators of immature Aedes fluviatilis (Diptera: Culicidae) and Biomphalaria glabrata (Mollusca: Planorbidae), Mem??rias do Instituto Oswaldo Cruz, vol.86, issue.4, pp.419-424, 1991.
DOI : 10.1590/S0074-02761991000400007

B. Hofkin, D. Hofinger, D. Koech, and E. Loker, : implications for the biological control of schistosomiasis, Annals of Tropical Medicine & Parasitology, vol.5, issue.6, 1992.
DOI : 10.1017/S0031182000059655

S. Sokolow, K. Lafferty, and A. Kuris, Regulation of laboratory populations of snails (Biomphalaria and Bulinus spp.) by river prawns, Macrobrachium spp. (Decapoda, Palaemonidae): Implications for control of schistosomiasis, Acta Tropica, vol.132, pp.64-74, 2014.
DOI : 10.1016/j.actatropica.2013.12.013

M. Zakikhani and M. Rau, Effects of Plagiorchis elegans (Digenea: Plagiorchiidae) Infection on the Reproduction of Biomphalaria glabrata (Pulmonata: Planorbidae), The Journal of Parasitology, vol.84, issue.5, pp.927-930, 1998.
DOI : 10.2307/3284622

C. Munoz-antoli, A. Marin, R. Toledo, and J. Esteban, Effect of Echinostoma friedi (Trematoda: Echinostomatidae) experimental infection on longevity, growth and fecundity of juvenile Radix peregra (Gastropoda: Lymnaeidae) and Biomphalaria glabrata (Gastropoda: Planorbidae) snails, Parasitology Research, vol.85, issue.6, pp.1663-1670, 2007.
DOI : 10.1007/s00436-007-0710-9

V. Tunholi-alves, V. Tunholi, D. Lustrino, L. Amaral, and S. Thiengo, Changes in the reproductive biology of Biomphalaria glabrata experimentally infected with the nematode Angiostrongylus cantonensis, Journal of Invertebrate Pathology, vol.108, issue.3, pp.220-223, 2011.
DOI : 10.1016/j.jip.2011.08.009

A. Van-den-hurk, S. Hall-mendelin, A. Pyke, F. Frentiu, and K. Mcelroy, Impact of Wolbachia on Infection with Chikungunya and Yellow Fever Viruses in the Mosquito Vector Aedes aegypti, PLoS Neglected Tropical Diseases, vol.5, issue.11, p.23133693, 2012.
DOI : 10.1371/journal.pntd.0001892.t002

L. Baton, E. Pacidonio, D. Goncalves, and L. Moreira, wFlu: characterization and evaluation of a native Wolbachia from the mosquito Aedes fluviatilis as a potential vector control agent, PLoS One, vol.8, p.23555728, 2013.

A. Burt, Heritable strategies for controlling insect vectors of disease, Phil Trans R Soc B, vol.369, 2014.

. St, R. Leger, and C. Wang, Genetic engineering of fungal biocontrol agents to achieve greater efficacy against insect pests, Applied Microbiology and Biotechnology, vol.85, pp.901-907, 2010.

H. Swamy, R. Asokan, P. Rajasekaran, R. Mahmood, and S. Nagesha, Analysis of Opportunities and Challenges in Patenting of Bacillus thuringiensis Insecticidal Crystal Protein Genes, Recent Patents on DNA & Gene Sequences, vol.6, issue.1, pp.64-71, 2012.
DOI : 10.2174/187221512799303181

C. Zhang, S. Zhang, J. Xia, F. Li, and W. Xia, The Immune Strategy and Stress Response of the Mediterranean Species of the Bemisia tabaci Complex to an Orally Delivered Bacterial Pathogen, PLoS ONE, vol.39, issue.4, p.24722540, 2014.
DOI : 10.1371/journal.pone.0094477.s005

J. Contreras, J. Mendoza, M. Martinez-aguirre, L. Garcia-vidal, and J. Izquierdo, Efficacy of Enthomopathogenic Fungus <I>Metarhizium anisopliae</I> Against <I>Tuta absoluta</I> (Lepidoptera: Gelechiidae), Journal of Economic Entomology, vol.107, issue.1, pp.121-124, 2014.
DOI : 10.1603/EC13404

D. Fischbein and J. Corley, Classical biological control of an invasive forest pest: a world perspective of the management of Sirex noctilio using the parasitoid Ibalia leucospoides (Hymenoptera: Ibaliidae), Bulletin of Entomological Research, vol.35, issue.01, pp.1-12, 2014.
DOI : 10.1016/B978-0-12-078148-5.50005-1

E. Stackebrandt, W. Frederiksen, G. Garrity, P. Grimont, and P. Kampfer, Report of the ad hoc committee for the re-evaluation of the species definition in bacteriology, Int J Syst Evol Microbiol, vol.52, pp.1043-1047, 2002.

D. Gevers, F. Cohan, J. Lawrence, B. Spratt, and T. Coenye, Opinion: Re-evaluating prokaryotic species, Nature Reviews Microbiology, vol.49, issue.9, pp.733-739, 2005.
DOI : 10.1128/AEM.71.2.930-939.2005

M. Gardener and B. , spp. in Agricultural Systems, Phytopathology, vol.94, issue.11, pp.1252-1258, 2004.
DOI : 10.1094/PHYTO.2004.94.11.1252

S. Lal and S. Tabacchioni, Ecology and biotechnological potential of Paenibacillus polymyxa: a minireview, Indian Journal of Microbiology, vol.22, issue.1, pp.2-10, 2009.
DOI : 10.1007/s12088-009-0008-y

R. Ivy, M. Ranieri, N. Martin, H. Bakker, and B. Xavier, Identification and Characterization of Psychrotolerant Sporeformers Associated with Fluid Milk Production and Processing, Applied and Environmental Microbiology, vol.78, issue.6, pp.1853-1864, 2012.
DOI : 10.1128/AEM.06536-11

T. Silva, E. Melo, A. Lopes, D. Veras, and C. Duarte, from Brazil, Letters in Applied Microbiology, vol.113, issue.1, pp.19-25, 2013.
DOI : 10.1111/lam.12068

URL : https://hal.archives-ouvertes.fr/hal-00404915

M. Heyndrickx, K. Vandemeulebroecke, B. Hoste, P. Janssen, and K. Kersters, Reclassification of Paenibacillus (formerly Bacillus) pulvifaciens (Nakamura 1984) Ash et al. 1994, a Later Subjective Synonym of Paenibacillus (formerly Bacillus) larvae (White 1906) Ash et al. 1994, as a Subspecies of P. larvae, with Emended Descriptions of P. larvae as P. larvae subsp. larvae and P. larvae subsp. pulvifaciens, International Journal of Systematic Bacteriology, vol.46, issue.1, pp.270-279, 1996.
DOI : 10.1099/00207713-46-1-270

H. Harrison, R. Patel, and A. Yousten, Paenibacillus Associated with Milky Disease in Central and South American Scarabs, Journal of Invertebrate Pathology, vol.76, issue.3, pp.169-175, 2000.
DOI : 10.1006/jipa.2000.4969

E. Genersch, American Foulbrood in honeybees and its causative agent, Paenibacillus larvae, Journal of Invertebrate Pathology, vol.103, pp.10-19, 2010.
DOI : 10.1016/j.jip.2009.06.015

I. Fries, A. Lindstrã-¶m, and S. Korpela, Vertical transmission of American foulbrood (Paenibacillus larvae) in honey bees (Apis mellifera), Veterinary Microbiology, vol.114, issue.3-4, pp.269-274, 2006.
DOI : 10.1016/j.vetmic.2005.11.068

A. Lindstrom, S. Korpela, and I. Fries, The distribution of Paenibacillus larvae spores in adult bees and honey and larval mortality, following the addition of American foulbrood diseased brood or spore-contaminated honey in honey bee (Apis mellifera) colonies, Journal of Invertebrate Pathology, vol.99, issue.1, pp.82-86, 2008.
DOI : 10.1016/j.jip.2008.06.010

E. Genersch, J. Evans, and I. Fries, Honey bee disease overview, Journal of Invertebrate Pathology, vol.103, pp.2-4, 2010.
DOI : 10.1016/j.jip.2009.07.015

E. Garcia-gonzalez, L. Poppinga, A. Funfhaus, G. Hertlein, and K. Hedtke, Paenibacillus larvae Chitin-Degrading Protein PlCBP49 Is a Key Virulence Factor in American Foulbrood of Honey Bees, PLoS Pathogens, vol.84, issue.7, p.25080221, 2014.
DOI : 10.1371/journal.ppat.1004284.t001

A. Crews and T. Yoshino, Schistosoma mansoni: Effect of infection on reproduction and gonadal growth in Biomphalaria glabrata, Experimental Parasitology, vol.68, issue.3, pp.326-334, 1989.
DOI : 10.1016/0014-4894(89)90114-8

M. Faro, M. Perazzini, C. Ldr, C. Mello-silva, and J. Pinheiro, Biological, biochemical and histopathological features related to parasitic castration of Biomphalaria glabrata infected by Schistosoma mansoni, Experimental Parasitology, vol.134, issue.2, pp.228-234, 2013.
DOI : 10.1016/j.exppara.2013.03.020

X. Huang, B. Tian, Q. Niu, Y. J. Zhang, and L. , An extracellular protease from Brevibacillus laterosporus G4 without parasporal crystals can serve as a pathogenic factor in infection of nematodes, Research in Microbiology, vol.156, issue.5-6, pp.719-727, 2005.
DOI : 10.1016/j.resmic.2005.02.006

T. Cheng, J. Sullivan, and K. Harris, Parasitic castration of the marine prosobranch gastropod Nassarius obsoletus by sporocysts of Zoogonus rubellus (Trematoda): Histopathology, Journal of Invertebrate Pathology, vol.21, issue.2, pp.183-190, 1973.
DOI : 10.1016/0022-2011(73)90200-0

S. Djordjevic, W. Forbes, L. Smith, and M. Hornitzky, Genetic and Biochemical Diversity among Isolates of Paenibacillus alvei Cultured from Australian Honeybee (Apis mellifera) Colonies, Applied and Environmental Microbiology, vol.66, issue.3, pp.1098-1106, 2000.
DOI : 10.1128/AEM.66.3.1098-1106.2000

C. Adema, C. Bayne, J. Bridger, M. Knight, and E. Loker, Will All Scientists Working on Snails and the Diseases They Transmit Please Stand Up?, PLoS Neglected Tropical Diseases, vol.130, issue.12, 2012.
DOI : 10.1371/journal.pntd.0001835